Supply Chain Project Manager, Rijswijk, Zuid-Holland

Company Overview Our client is a leading innovator in health technology, dedicated to developing advanced medical solutions that enhance patient care and improve health outcomes. They operate globally, integrating cutting-edge research and development to push the boundaries of medical device innovation. Job Description We are seeking a talented Computational Modeling Engineer to join the firm’s Innovation and Design team. In this role, you will apply your expertise in physics, mechanics, or computational modeling to support the development of new medical devices. Your work will focus on creating virtual prototypes and simulations to provide physical insights and predictive data, helping to streamline product development and reduce risk. Responsibilities Contribute to R&D projects by developing and running advanced computational simulations. Develop, validate, and apply physics-based models to optimize design decisions. Strengthen the team’s expertise in computational (bio)physics. Keep up-to-date with the latest modeling techniques and simulation tools. Support innovation initiatives in image-guided therapy, diagnostics, patient monitoring, and personal care by translating application needs into suitable modeling strategies. Requirements -Preferably a PhD in Mechanical Engineering, Applied Physics, or a related field, with experience in computational modeling. -Solid understanding of physics-based modeling of solid mechanics or dynamics. -Experience translating simulation results into insights for engineering and R&D teams. -Curious, innovative, and analytical mindset. -Proactive, flexible, and able to take ownership of technical challenges. -Experience with commercial or open-source simulation tools such as ANSYS, Abaqus, OpenFOAM, or Comsol is advantageous. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company: Our client is a leading organization in the pharmaceutical industry, dedicated to ensuring the highest standards of product quality and compliance. They operate within a heavily regulated environment, committed to delivering safe and effective medicines to the market. Job Description: We are seeking an experienced Quality Assurance Specialist to oversee the release of pharmaceutical products, ensuring all are compliant with applicable laws, regulations, and internal standards. This key role involves inspecting, reviewing, and authorizing product documentation, managing quality investigations, and supporting regulatory inspections. Responsibilities: •    Review and approve master documents and specifications to support product release. •    Initiate and evaluate quality investigations, including deviations, to determine release or rejection, and implement improvement proposals. •    Ensure timely completion of deviation and investigation reports. •    Lead quality improvement initiatives to control production risks. •    Authorize ongoing stability studies and Product Quality Reviews. •    Prepare for and oversee inspections by government agencies and customers. •    Participate in self-inspections across production, laboratory, storage, and distribution areas. •    Support and coordinate handling of complaints, root cause analysis, and implementation of corrective actions. •    Manage product recalls and stock blockage proposals. •    Investigate and document deviations and complaints thoroughly. •    Develop and maintain relationships with external partners related to quality oversight. •    Participate in technology transfer activities and contribute to process improvements. •    Provide functional leadership to QA team members, including organizing work, implementing structured procedures, and contributing to staffing and training decisions. Requirements: •    Degree in pharmacy, chemistry, biology, or a related field (per EU Directive 2001/83/EC). •    Extensive experience with aseptic manufacturing processes (preferably over 5 years). •    Knowledge of lyophilization and visual inspection processes is a plus. •    Familiarity with automated pharmaceutical processes. •    Strong understanding of EU and US pharmaceutical laws and regulations. •    Proficient in analytical methods. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview Our client is a dynamic organization operating within the manufacturing and logistics industry in the Netherlands. They are dedicated to delivering high-quality products through efficient supply chain management and innovative operational practices. Job Description We are seeking an experienced Co-Packing Operations Lead to support and oversee ongoing co-packing activities across the Benelux region. This pivotal role involves stabilizing daily operations, managing risks, and ensuring continuity while conducting a comprehensive review of the co-packing scope to optimize processes, capacity, and resource allocation. Responsibilities -Ensure the smooth execution of daily co-packing activities across the Benelux region, acting as the main operational contact and addressing urgent issues promptly. -Collaborate with Logistics, Planning, Customer Service, Marketing, Procurement, Quality teams, and external partners to support operational needs and governance. -Maintain transparency on requests, priorities, owners, deadlines, dependencies, and status updates. -Organize and lead governance meetings and decision-making forums to facilitate effective communication and issue resolution. -Manage accurate administrative records, including instruction cards, specifications, price lists, supplier info, and decision logs. -Coordinate master data, material administration, purchase orders, system updates, and escalation procedures, ensuring system transmission and operational priorities are aligned. -Conduct a comprehensive inventory of current co-packing activities, measuring effort, frequency, seasonality, and complexities to determine current and future capacity needs. -Identify quick wins and strategic opportunities to improve process reliability, reduce costs, and enhance sustainability. -Document and implement feasible improvements, creating a roadmap for ongoing enhancements and a smooth handover. Requirements -Strong background in supply chain, logistics, co-packing, or operational project management. -Ability to quickly understand complex processes and operational constraints. -Excellent analytical skills, including process mapping and capacity assessment. -Confident stakeholder management and communication skills. -Experience with continuous improvement initiatives and organizational assessments. -Knowledge of SAP, co-packing operations, or excise processes is a plus. -Skilled in using SAP and Microsoft 365 for purchase orders, master data management, reporting, and documentation. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The Company The client is one of the Netherlands’ biggest dairy products manufacturers who is also active globally.    Role Description As the MRP Lead you will lead a team of three Material Requirements Planning (MRP) professionals responsible for ensuring the timely availability of raw materials and packaging components for production sites in Meppel and Lippstadt. The role combines people leadership, supply planning expertise, supplier management, and tactical supply chain oversight. You will be part of the Encaps Supply Team, a global leader in dairy and plant-based ingredient solutions. In this position, you will ensure optimal material availability, support business continuity, drive supplier performance, and contribute to achieving the right balance between cost, service, and inventory levels. The role requires both operational involvement and a tactical outlook, partnering closely with suppliers, procurement, production, and other key stakeholders. Responsibilities Lead and coach a team of three Material Planners. Support team members in managing priorities, resolving issues, and handling escalations. Facilitate regular team check-ins and performance discussions. Foster professional growth and continuous development within the team. Oversee the end-to-end planning and ordering process for raw materials and packaging materials. Ensure material availability to support uninterrupted production and delivery performance. Adjust planning activities in response to changing production schedules and demand requirements. Forecast material requirements based on supply and production plans. Monitor and optimize inventory levels while balancing working capital and service performance. Build and maintain strong relationships with suppliers and internal stakeholders. Conduct tactical supplier performance reviews and drive continuous improvements. Manage supplier escalations and support resolution of supply-related issues. Collaborate with Procurement on long-term volume planning, contract coverage, and supply continuity strategies. Develop contingency plans and alternative sourcing options to mitigate supply risks. Own and monitor key MRP performance indicators, including Supplier OTIF and Raw & Packaging Inventory Value. Identify opportunities to improve planning processes, supplier performance, and operational efficiency. Challenge existing ways of working and implement sustainable improvements. Contribute to strategic and tactical supply chain initiatives beyond day-to-day operations. Requirements Bachelor's degree (HBO/University level) in Supply Chain Management, Logistics, Business Administration, or a related field. Experience in Supply Planning, Material Planning, ERP Planning, or a similar supply chain role. Previous leadership or team coordination experience is preferred, ideally around one year or more. Knowledge of manufacturing and supply chain processes. Strong SAP proficiency. Good understanding of inventory management, material planning, and supplier performance management. Experience working in complex, fast-paced production environments. Strong communication and stakeholder management skills. Proactive, hands-on, and solution-oriented mindset. Ability to escalate issues effectively and manage supply risks in a Just-in-Time (JIT) environment. Customer-focused with a strong drive for operational excellence. Commercially aware with a clear understanding of cost and working capital impacts. Continuous improvement mindset with the confidence to challenge the status quo. Strong team player capable of operating across multiple stakeholders and functions. Able to balance operational execution with tactical and longer-term planning horizons. Fluent in Dutch and English. German language skills are considered an advantage. Willingness to travel regularly to Meppel (approximately once per week) and occasionally to Lippstadt (approximately once every 1-2 months). Based primarily in Amersfoort with a hybrid working arrangement. Other Information Apply to our vacancy for more information. Looking forward to getting in touch! 

The Company A global pharmaceutical organization focused on science driven innovation, technology excellence, and high quality manufacturing. The company operates across international markets and collaborates closely with manufacturing sites, technical operations teams, and external manufacturing partners to deliver compliant and efficient product supply. Role description The Technology Transfer Program Manager is responsible for leading Small Molecule drug product technology transfer projects across manufacturing sites. The role provides end to end oversight of transfer execution, ensuring projects are delivered on time, within quality standards, and in compliance with GMP and regulatory requirements. This position works closely with internal stakeholders, manufacturing facilities, contract manufacturing organizations, and global teams to drive successful technology transfer outcomes while continuously improving transfer methodologies and governance processes. Responsibilities - Lead and coordinate multiple Small Molecule technology transfer projects simultaneously - Manage site to site transfer execution activities across manufacturing networks - Monitor project timelines, milestones, risks, and project performance metrics - Ensure transfers are completed according to quality, compliance, and regulatory requirements - Coordinate activities between donor and receiving manufacturing sites - Collaborate with Manufacturing, Quality, Regulatory, Supply Chain, Procurement, Finance, PTS, and ATS teams - Facilitate stakeholder alignment on project objectives and deliverables - Act as the primary point of contact for technology transfer activities - Develop and maintain governance frameworks and project reporting structures - Coach project teams and support transfer sponsors throughout project execution - Support regulatory submission activities related to technology transfers - Assist with process validation, qualification, and technical documentation - Drive continuous improvement initiatives and technology transfer best practices - Provide expertise in technical problem solving and issue resolution Requirements - Bachelor of Science degree in Engineering, Chemistry, Biology, or a related scientific discipline - More than 10 years of experience in Technology Transfer, Product Development, Manufacturing Operations, or Technical Operations - Strong experience with Small Molecule pharmaceutical products - Knowledge of liquids, ointments, creams, sterile injectables, sterile pastes, and powder filling processes - Strong understanding of EU and FDA GMP regulations - Experience with change control, deviation management, technical protocols, and technical reports - Experience with regulatory licensing documentation - Expert level project management and project controlling skills - Advanced stakeholder management and communication skills - Experience working within complex matrix organizations - Ability to lead cross functional teams without direct authority - Strong negotiation and influencing capabilities - Experience using Microsoft Project and enterprise project management tools - Fluent English communication skills - Experience working with multicultural and geographically diverse teams - Knowledge of German or French is an advantage Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me

Company  A leading organization in the pharmaceutical industry dedicated to ensuring the highest quality standards in manufacturing and product development. The company operates under strict regulatory guidelines and values excellence, compliance, and continuous improvement. Role Description We are looking for an experienced Quality Assurance Specialist Qualified Person (QP) to oversee and ensure the quality and regulatory compliance of pharmaceutical products. This role involves coordinating product release, managing quality investigations, and supporting inspections and audits to uphold the company’s high standards in production. Responsibilities - Review and approve master documents and specifications to ensure compliance - Initiate and evaluate quality investigations, making release or rejection decisions, and implementing improvement actions - Complete deviation and investigation reports promptly and accurately - Lead quality improvement initiatives to mitigate risks in production processes - Authorize ongoing stability studies and product quality reviews - Prepare for and manage inspections by government agencies and customers, including self-inspections and participation in overseas audits - Handle product complaints, investigate causes, and coordinate recalls when necessary - Maintain communication with external regulators, clients, and partners - Support technology transfer activities and ensure smooth knowledge transfer processes - Provide functional leadership to QA team members, including planning, structuring, and training staff Requirements - Degree in pharmacy, chemistry, biology, or a related field (per art 49 paragraph 2 directive 2001/83/EC) - Over 5 years of experience in aseptic production, with knowledge of lyophilization and visual inspection preferred - Strong understanding of pharmaceutical laws and regulations (EU and US) - Proficiency in analytical methods and automated processes - Decisive, results-oriented, and transparent communicators with a proactive approach Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company  Our client is a well-established, international food production and ingredients organisation with multiple manufacturing sites in Europe. They operate in a fast-paced supply chain environment where service, quality, and continuity of production are critical. The culture is professional, collaborative, and focused on continuous improvement. Job Description  For our client, we are looking for a Materials Planner to lead a small European materials planning team and ensure the timely availability of raw and packaging materials for production. The Materials Planning Team Lead (SAP) balances day-to-day operational priorities with a more tactical, forward-looking approach, working closely with internal stakeholders and suppliers to protect supply continuity. Responsibilities  - Lead and support a small materials planning team responsible for raw and packaging material availability across multiple production sites. - Manage the end-to-end ordering process for materials, ensuring orders are placed accurately and on time. - Monitor and optimise inventory levels while supporting working capital targets. - Translate production plans into material requirements and adjust plans when schedules change. - Coordinate and resolve supplier-related issues, including delivery problems and purchase complaints. - Ensure accurate order handling and invoice control in collaboration with relevant internal teams. - Drive performance management for the materials planning scope, including supplier delivery performance (e.g., OTIF) and inventory value. - Prepare and run structured supplier performance reviews and align on improvement actions. - Build and maintain contingency approaches to reduce risk and improve supply reliability. - Support escalations when supply risks impact production, and align actions with key stakeholders. - Identify improvement opportunities and take ownership for implementing practical solutions. Requirements  - Bachelor-level education (Supply Chain, Logistics, or a related field). - Strong experience in materials planning / supply planning / ERP planning. - Proven ability to lead, guide, or coach a team (formal people leadership is a plus). - Solid SAP proficiency (required). - Fluent in Dutch and English (German is a plus). - Strong communication skills and confident stakeholder management. - Proactive, improvement-minded, and able to challenge the status quo constructively. - Willingness to travel regularly to a Dutch production site and occasionally to a German site. - Temporary Full-Time Contract (6 Months) Other Information The role is based in the Netherlands with a mix of on-site and hybrid working, depending on business needs. Regular interaction with production, procurement, and suppliers is key, and the successful candidate will be comfortable operating in a time-sensitive supply environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading organization in the pharmaceutical industry dedicated to the development and manufacturing of Small Molecule drug products. They prioritize innovation, quality, and regulatory compliance to deliver high-quality medicines to patients worldwide. Job Description We are seeking an experienced Senior Project Manager to lead and oversee large-scale Small Molecule drug product technology transfers across manufacturing sites. The role involves managing key projects from start to finish, ensuring timely complaints, and high-quality transfer execution to support the company's strategic growth. Responsibilities -Lead multiple Small Molecule technology transfer projects, ensuring smooth site-to-site transfers. -Oversee project timelines, risks, and milestones via dashboards and reporting tools. -Collaborate closely with Manufacturing, Quality, Regulatory, Supply Chain, Procurement, and other teams to align project goals and resolve issues. -Develop and maintain project governance, provide best practices, and coach project teams and sponsors. -Act as the primary contact for manufacturing sites and global functions, fostering strong relationships and clear communication. -Support regulatory submissions related to transfers and ensure compliance with GMP standards. -Contribute to continuous improvement of transfer processes and methodologies, driving best practices across regions. -Provide technical expertise and support for resolving transfer-related challenges. -Perform additional duties as assigned by management. Requirements -Bachelor’s degree or higher in Engineering, Chemistry, Biology, or a relevant scientific discipline. -Over 5+ years of experience in technology transfer, product development, or manufacturing operations within the pharmaceutical industry. -Extensive knowledge of Small Molecule drug product types, including liquids, ointments, creams, sterile injectables, and powders. -Proven ability to manage complex projects, with experience using enterprise project management tools like MS Project. -Strong knowledge of GMP regulations and regulatory processes, especially for EU and FDA standards. -Excellent stakeholder management, communication, and leadership skills. -Fluent in English, with additional language skills (e.g., German or French) considered an advantage. -Willingness to travel internationally approximately 10-20%. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company Our client is a leading global pharmaceutical organization focused on innovation, scientific excellence, and the reliable delivery of high-quality medicines. The organization operates across international manufacturing sites and maintains strong standards for GMP, regulatory compliance, and operational excellence. Role Description As an Associate Director, Technology Transfer Execution, you are responsible for leading Small Molecule technology transfer projects across global manufacturing sites, managing transfer execution from planning through completion while ensuring projects are delivered on time, in compliance with GMP and regulatory requirements, and to the required quality standards. You will work closely with Manufacturing, Quality, Regulatory Affairs, Supply Chain, Technical teams, CMOs, and global stakeholders to ensure successful project execution and alignment. Responsibilities - Lead and coordinate multiple Small Molecule technology transfer projects across manufacturing sites. - Manage project timelines, milestones, risks, deliverables, and governance. - Coordinate activities between donor and receiving sites and ensure effective stakeholder alignment. - Work cross-functionally with Manufacturing, Quality, Regulatory, Supply Chain, and Technical teams. - Support GMP compliance, process validation, qualification, change controls, deviations, and regulatory documentation. - Act as a key contact for manufacturing sites, global stakeholders, and CMOs. - Provide guidance, coaching, and problem-solving support to transfer teams. - Drive continuous improvement of technology transfer processes and best practices. - Communicate project progress, risks, and challenges to senior stakeholders. - Travel internationally approximately 10–20% of the time. Requirements - Bachelor’s degree in Engineering, Chemistry, Biology, or a related technical/scientific field. - 10+ years of experience in Technology Transfer, Product Development, Manufacturing Operations, or Technical Operations within pharmaceuticals. - Strong experience with Small Molecule pharmaceutical products and manufacturing processes. - Strong knowledge of GMP and EU/FDA regulatory requirements. - Experience with technology transfer, process validation, qualification, change control, and deviation management. - Strong project management and stakeholder management skills. - Experience working in global, cross-functional, and matrix environments. - Excellent English communication, negotiation, and influencing skills. - Proficiency with MS Project and Microsoft Office; SAP knowledge is an advantage. - Willingness to travel internationally 10–20%. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company Our client is a leading organization committed to maintaining the highest standards in quality and compliance within their regulated operations. They focus on ensuring safe and effective products through meticulous documentation and adherence to GMP guidelines. Role Description As a QA Documentation Specialist, you are responsible for verifying the accuracy and completeness of controlled batch documents and labels, ensuring compliance with quality standards and regulatory requirements, and supporting continuous improvement of documentation processes. Responsibilities - Verify controlled batch documents and label packages, including final product labels, in accordance with cGMP standards. - Confirm the accuracy and completeness of QA-issued documents and logbooks. - Ensure timely use and proper management of GMP materials and consumables, informing the responsible personnel as needed. - Identify and escalate compliance issues within the controlled issuance process. - Support initiatives aimed at improving documentation procedures. - Investigate deviations related to controlled document issuance and develop effective corrective action plans. - Perform additional duties as assigned, delegating tasks to qualified team members when necessary. - Prioritize tasks to meet deadlines, demonstrating strong attention to detail and accuracy. - Communicate effectively with colleagues at all levels, including senior stakeholders, and cross-train peers on documentation procedures. - Maintain advanced technical knowledge of GMP processes and ensure clear presentation of documentation operations and guidelines. Requirements - HBO or WO level education. - At least 2 years of experience managing documents in a regulated environment. - Strong command of English communication, both written and verbal. - Positive attitude and a detail-oriented approach. - Ability to work within a structured schedule, including working on weekends in a rotational pattern every six weeks, with adequate rest days. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.